A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628281



Internal ID21576586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118940825..118940825hg38UCSC Ensembl
chr6:119261990..119261990hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139632
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628281
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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